Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g05620 | A01 | 2477573 | C | T | upstream_gene_variant | MODIFIER | c.-3780C>T| |
S2 |
2 | BAA01g05620 | A01 | 2478834 | G | A | upstream_gene_variant | MODIFIER | c.-2519G>A| |
S259 |
3 | BAA01g05620 | A01 | 2479218 | C | T | upstream_gene_variant | MODIFIER | c.-2135C>T| |
S97 |
4 | BAA01g05620 | A01 | 2483597 | G | A | missense_variant | MODERATE | c.1616G>A|p.Arg539Lys |
S183 S198 |
5 | BAA01g05620 | A01 | 2484000 | G | A | synonymous_variant | LOW | c.2019G>A|p.Glu673Glu |
S136 |
6 | BAA01g05620 | A01 | 2484578 | C | T | missense_variant | MODERATE | c.2333C>T|p.Ser778Phe |
S18 |
7 | BAA01g05620 | A01 | 2484637 | G | A | missense_variant | MODERATE | c.2392G>A|p.Gly798Arg |
S116 |
8 | BAA01g05620 | A01 | 2485146 | G | A | missense_variant | MODERATE | c.2794G>A|p.Ala932Thr |
S201 |
9 | BAA01g05620 | A01 | 2485247 | C | T | synonymous_variant | LOW | c.2895C>T|p.Tyr965Tyr |
S218 |
10 | BAA01g05620 | A01 | 2485268 | C | T | synonymous_variant | LOW | c.2916C>T|p.His972His |
S54 |
11 | BAA01g05620 | A01 | 2489824 | C | T | missense_variant | MODERATE | c.5243C>T|p.Ala1748Val |
S62 |
12 | BAA01g05620 | A01 | 2492436 | G | A | downstream_gene_variant | MODIFIER | c.*1662G>A| |
S197 |
13 | BAA01g05620 | A01 | 2494048 | G | A | downstream_gene_variant | MODIFIER | c.*3274G>A| |
S292 |